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FDA 510(k), K020608, HD/HDT, (POLYMACON) SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND TINTED, FULLY CAST-MOLDED LENS)
FDA 510(k), K020608, HD/HDT, (POLYMACON) SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND TINTED, FULLY CAST-MOLDED LENS)
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510(K) Number: K020608
Device Name: HD/HDT, (POLYMACON) SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND TINTED, FULLY CAST-MOLDED LENS)
Manufacturer: POLY VUE TECHNOLGIES, INC.
Device Classification Name: Lenses, Soft Contact, Daily Wear
Regulation Number: 886.5925
Classification Product Code: LPL
Date Received: 02/25/2002
Decision Date: 05/16/2002
Regulation Medical Specialty: Ophthalmic
Device Name: HD/HDT, (POLYMACON) SOFT CONTACT LENS FOR DAILY WEAR (CLEAR AND TINTED, FULLY CAST-MOLDED LENS)
Manufacturer: POLY VUE TECHNOLGIES, INC.
Device Classification Name: Lenses, Soft Contact, Daily Wear
Regulation Number: 886.5925
Classification Product Code: LPL
Date Received: 02/25/2002
Decision Date: 05/16/2002
Regulation Medical Specialty: Ophthalmic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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